Summary | Mutation origin | Mutation description | Phenotypes | Find Mice (IMSR) | References

Symbol:	T22H
Name:	brachyury, T-box transcription factor T; brachyury 22 Harwell
MGI ID:	MGI:1857529
Synonyms:	Del(17)T22H, Del(17)T22H11H
Gene:	T  Location: Chr17:8653255-8661328 bp, + strand  Genetic Position: Chr17, 4.92 cM
Alliance:	T22H page

Strain of Origin:

(C3H/HeH x 101/H)F1

Allele Type:    Radiation induced Mutation:    Deletion   T22H involves 1 genes/genome features (T) View all   Mutation details: G-banded mitotic chromosome preparations show significant shortening of band 17A3. This allele comprises a deletion with a proximal breakpoint distal to D17Mit245 and a distal breakpoint proximal to D17Mit156. Loci D17Mit19 and 164, D17Tu1, and T are known to be deleted. (J:62654, J:62655) Inheritance:    Semidominant

View phenotypes and curated references for all genotypes (concatenated display).

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any T Mutation:	60 strains or lines available

Original:	J:11036 Howard CA, et al., Genetic and molecular analysis of the proximal region of the mouse t-complex using new molecular probes and partial t-haplotypes. Genetics. 1990 Dec;126(4):1103-14
All:	5 reference(s)